scholarly journals Optical Characterization of Chemically Etched Nanoporous Silicon Embedded in Sol-Gel Matrix

2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
A. S. Al Dwayyan ◽  
M. Naziruddin Khan ◽  
M. S. Al Salhi
Keyword(s):  
Electron Microscopy ◽  
Sol Gel ◽  
Spherical Shape ◽  
Nanoporous Silicon ◽  
Transmission Electron ◽  
Sol Gel Process ◽  
Si Nanoparticles ◽  
The Matrix ◽  
Crystalline Nature

Nanoporous (NPs) silicon fabricated by chemical etching process in HF acid was first separated in tetrahydrofuran (THF) solvent and then incorporated into SiO2matrix. The matrix was prepared by sol gel process in which dimethylformamide (DMF) was used as drying chemical control additive (DCCA) to form crack-free dried sample. We examined the optical properties of NPs in three medium which are solvent, sol, and dried sol gel. Our observations reveal that absorption spectra of NPs silicon in THF are modified with respect to the spectra in sol gel. Significant stability in PL of NPs silicon in the sol gel is observed. Influence of matrix environment on peaks of NPs is also discussed. Surface morphology is characterized by field emission scanning electron microscopy (FESEM) which shows that the NPs silicon in THF is similar to the sol gel but becomes aggregation particle to particle. Presence of Si nanoparticles in THF and sol is confirmed by Transmission electron microscopy (TEM). The NPs silicons have mono dispersive and high crystalline nature with spherical shape of around 5 nm in sizes.

Synthesis and Characterization of SiO2@Y2MoO6:Eu3+ Core–Shell Structured Spherical Phosphors by Sol–Gel Process

2016 ◽  
Vol 16 (4) ◽  
pp. 3914-3920 ◽  
Author(s):  
G. Z Li ◽  
F. H Liu ◽  
Z. S Chu ◽  
D. M Wu ◽  
L. B Yang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Annealing Temperature ◽  
Uv Light ◽  
Sol Gel ◽  
Spherical Shape ◽  
Core Shell ◽  
X Ray ◽  
Transmission Electron ◽  
Sol Gel Process ◽  
Average Size

SiO2@Y2MoO6:Eu3+ core–shell phosphors were prepared by the sol–gel process. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectra (EDS), transmission electron microscopy (TEM), photoluminescence (PL) spectra as well as kinetic decays were used to characterize the resulting SiO2@Y2MoO6:Eu3+ core–shell phosphors. The XRD results demonstrated that the Y2MoO6:Eu3+ layers on the SiO2 spheres crystallized after being annealed at 700 °C and the crystallinity increased with raising the annealing temperature. The obtained core–shell phosphors have spherical shape with narrow size distribution (average size ca. 640 nm), non-agglomeration, and smooth surface. The thickness of the Y2MoO6:Eu3+ shells on the SiO2 cores could be easily tailored by varying the number of deposition cycles (70 nm for four deposition cycles). The Eu3+ shows a strong PL emission (dominated by 5D0–7F2 red emission at 614 nm) under the excitation of 347 nm UV light. The PL intensity of Eu3+ increases with increasing the annealing temperature and the number of coating cycles.

Sol-gel Elaboration of Porous Oxide Coatings as Interphase in SiC/SiC Ceramic Matrix Composites

2003 ◽  
Vol 775 ◽  
Author(s):  
M. Verdenelli ◽  
S. Parola ◽  
F. Chassagneux ◽  
S. Jacques ◽  
H. Vincent ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Sol Gel ◽  
Ceramic Matrix Composites ◽  
Matrix Composites ◽  
X Ray Diffraction ◽  
Brittle Behavior ◽  
Transmission Electron ◽  
Sol Gel Process ◽  
The Matrix ◽  
Mesoporous Oxide

AbstractCombinations of meso-, macro- and microporous coatings with a chemical composition of 90%Al2O3-10%SiO2 were elaborated on SiC Hi-Nicalon fibers using the sol-gel process. They were evaluated as porous interphase for the reinforcement of CMC. The mesoporous oxide, in contact with the fiber, allows cracks deviation whereas the macroporous one, in contact with the matrix, avoids the gaseous infiltration of the mesopores during the SiC CVD matrix process. It also prevents from oxygen diffusion during high temperature under air. The characterization of the composites was performed by SEM (scanning electron microscopy), TEM (transmission electron microscopy), X-ray diffraction, and EDS (energy dispersive spectrometry). TEM evidenced the porosity gradient as expected. A tensile test on the composites revealed brittle behavior (fracture) and no fiber debonding was observed.

scholarly journals Synthesize and Characterization of Hollow Boron-Nitride Nanocages

2009 ◽  
Vol 2009 ◽  
pp. 1-4 ◽  
Author(s):  
W. S. Zhang ◽  
J. G. Zheng ◽  
W. F. Li ◽  
D. Y. Geng ◽  
Z. D. Zhang
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
High Resolution ◽  
Boron Nitride ◽  
Growth Mechanism ◽  
Spherical Shape ◽  
Amorphous Boron ◽  
Transmission Electron ◽  
Ammonia Atmosphere

The boron-nitride (BN) nanocages are synthesized by nitrogenation of amorphous boron nanoparticles at 1073 K under nitrogen and ammonia atmosphere. The BN nanocages exhibit a well-crystallized feature with nearly pentagonal or spherical shape, depending on their size. High-resolution transmission electron microscopy studies reveal that they are hollow nanocages. The growth mechanism of the BN nanocages is proposed.

Characterization of Nanostructured Silica as Carrier for Insecticides Deltamethrin, Pyriproxyfen, and Chlorpyrifos and Testing the Insecticidal Efficacy Against Trogoderma granarium (Coleoptera: Dermestidae) Larvae

2019 ◽  
Vol 113 (1) ◽  
pp. 511-517
Author(s):  
Masumeh Ziaee ◽  
Asgar Babamir-Satehi
Keyword(s):  
Electron Microscopy ◽  
Silica Nanoparticles ◽  
Sol Gel ◽  
Sem Analysis ◽  
Efficient Treatment ◽  
Trogoderma Granarium ◽  
Transmission Electron ◽  
Insecticidal Efficacy ◽  
Sol Gel Process ◽  
Nanostructured Silica

Abstract Nanostructured silica can be used as a carrier of pesticides to enhance stability and controlled release of agrochemicals with an effective concentration on target pests. Silica nanoparticles (SNPs) were synthesized by sol–gel process and employed as a carrier of three different insecticides including deltamethrin, pyriproxyfen, and chlorpyrifos. The SNPs were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM) analysis and the insecticides-loaded in SNPs were characterized by transmission electron microscopy (TEM). The toxicity of insecticides alone and loaded in SNPs was evaluated against small and large larvae of Trogoderma granarium Everts on concrete surfaces. The immediate mortality was counted after 1, 3, and 7 d of exposure, and then surviving individuals were transferred to untreated surfaces for seven more days, with delayed mortality was recorded. Small larvae were more susceptible than large ones on all insecticide treatments. In addition, insecticides loaded in silica nanoparticles were more effective when compared with application of the insecticides alone. For immediate mortality, deltamethrin loaded in SNPs was the most efficient treatment causing 70.5% mortality on small and 55.5% mortality on large larvae after 7 d of exposure to the highest concentration. Pyriproxyfen loaded in SNPs caused low immediate mortality, but the mortality increased in delayed count indicated that the insecticide could control the larvae even after they have been removed from treated surfaces. It can be concluded that loading insecticides in SNPs could significantly increase their insecticidal efficiency, but this increase was compound-dependent.

Synthesis and Characterization of Thiol- and Carboxyl-Functionalized Mesoporous Silica Nanoparticles

2017 ◽  
Vol 1142 ◽  
pp. 220-224 ◽  
Author(s):  
Wan Xia Wang ◽  
Yu Wang ◽  
Hua Meng Gong ◽  
Hong Hao Sun ◽  
Ming Xing Liu
Keyword(s):  
Electron Microscopy ◽  
Mesoporous Silica ◽  
Silica Nanoparticles ◽  
Mesoporous Silica Nanoparticles ◽  
Spherical Shape ◽  
Synthesis And Characterization ◽  
Functionalized Mesoporous Silica ◽  
Transmission Electron ◽  
Ft Ir

The purpose of this article is to synthesize the thiol-and carboxyl-bifunctionalized mesoporous silica nanoparticles (CMS-SH-COOH). CMS-SH-COOH was successfully synthesized by co-condensation and post-grafting methods. Moreover, the particle size and structural properties of CMS-SH-COOH were characterized by transmission electron microscopy (TEM), dynamic light scattering (DLS) and Fourier transform infrared spectroscopy (FT-IR). The obtained results indicated that the CMS-SH-COOH presented a uniform spherical shape with a wormhole arrangement of the mesopores and a relatively narrow paticle distribition. Therefore, the CMS-SH-COOH might be a great potential carrier for the drug delivery system in the future.

scholarly journals Fabrication of TiO2Nanotanks Embedded in a Nanoporous Alumina Template

2015 ◽  
Vol 2015 ◽  
pp. 1-7 ◽  
Author(s):  
C. Massard ◽  
S. Pairis ◽  
V. Raspal ◽  
Y. Sibaud ◽  
K. O. Awitor
Keyword(s):  
Electron Microscopy ◽  
Sol Gel ◽  
Thermal Treatments ◽  
X Ray Diffraction ◽  
Alumina Template ◽  
Nanoporous Alumina ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Sol Gel Process

The feasibility of surface nanopatterning with TiO2nanotanks embedded in a nanoporous alumina template was investigated. Self-assembled anodized aluminium oxide (AAO) template, in conjunction with sol gel process, was used to fabricate this nanocomposite object. Through hydrolysis and condensation of the titanium alkoxide, an inorganic TiO2gel was moulded within the nanopore cavities of the alumina template. The nanocomposite object underwent two thermal treatments to stabilize and crystallize the TiO2. The morphology of the nanocomposite object was characterized by Field Emission Scanning Electron Microscopy (FESEM). The TiO2nanotanks obtained have cylindrical shapes and are approximately 69 nm in diameter with a tank-to-tank distance of 26 nm. X-ray diffraction analyses performed by Transmission Electron Microscopy (TEM) with selected area electron diffraction (SAED) were used to investigate the TiO2structure. The optical properties were studied using UV-Vis spectroscopy.

Microstructural characteristics and photoluminescence performance of nanograined thermally treated CeO2-TiO2 xerogels

2007 ◽  
Vol 22 (5) ◽  
pp. 1182-1187
Author(s):  
Amita Verma ◽  
A.K. Srivastava ◽  
N. Karar ◽  
Harish Chander ◽  
S.A. Agnihotry
Keyword(s):  
Electron Microscopy ◽  
Crystallite Size ◽  
Sol Gel ◽  
Structural Features ◽  
X Ray Diffraction ◽  
Molar Ratios ◽  
Transmission Electron ◽  
Sol Gel Process ◽  
Crystallite Sizes ◽  
Thermally Treated

Nanostructured thermally treated xerogels have been synthesized using a sol-gel process involving cerium (Ce) chloride heptahydrate and titanium (Ti) propoxide mixed in different Ce:Ti molar ratios. Structural features of the xerogels have been correlated with their photoluminescence (PL) response. The crystallite sizes in the samples lie in the nanorange. The x-ray diffraction and transmission electron microscopy results have confirmed the coexistence of CeO2 and TiO2 nanocrystallites in these xerogels. In general, a decrease in the CeO2 crystallite size and an increase in the TiO2 crystallite size are observed in the xerogels as a function of Ti content. Scanning electron microscopy results have evidenced the evolution of ordered structure in the xerogels as a function of TiO2 content. Although both of the phases (CeO2 and TiO2) have exhibited PL in ultraviolet and visible regions, the major luminescence contribution has been made by the CeO2 phase. The largest sized CeO2 crystallites in 1:1 thermally treated xerogel have led to its highest PL response. PL emission in the xerogels is assigned to their nanocrystalline nature and oxygen vacancy-related defects.

Sol-gel derived Ba(Mg1/3Ta2/3)O3 thin films: Preparation and structure

1997 ◽  
Vol 12 (3) ◽  
pp. 596-599 ◽  
Author(s):  
Ji Zhou ◽  
Qing-Xin Su ◽  
K. M. Moulding ◽  
D. J. Barber
Keyword(s):  
Thin Films ◽  
Annealing Temperature ◽  
Volume Fraction ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Sol Gel Process ◽  
Small Grains

Ba(Mg1/3Ta2/3)O3 thin films were prepared by a sol-gel process involving the reaction of barium isopropoxide, tantalum ethoxide, and magnesium acetate in 2-methoxyethanol and subsequently hydrolysis, spin-coating, and heat treatment. Transmission electron microscopy, x-ray diffraction, and Raman spectroscopy were used for the characterization of the thin films. It was shown that the thin films tend to crystallize with small grains sized below 100 nm. Crystalline phase with cubic (disordered) perovskite structure was formed in the samples annealed at a very low temperature (below 500 °C), and well-crystallized thin films were obtained at 700 °C. Although disordered perovskite is dominant in the thin films annealed below 1000 °C, a low volume fraction of 1 : 2 ordering domains was found in the samples and grows with an increase of annealing temperature.

TEM Study of Rutile-Phase TiO2 Nanosheets

2013 ◽  
Vol 850-851 ◽  
pp. 156-159
Author(s):  
Xin Yan Wu ◽  
Wei Xiong
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Photocatalytic Activity ◽  
Energy Dispersive Spectrometer ◽  
Sol Gel ◽  
Rutile Phase ◽  
High Photocatalytic Activity ◽  
X Ray ◽  
Transmission Electron ◽  
Sol Gel Process

TiO2 nanosheets have been successfully synthesized via a simple sol-gel process. These nanostructures were characterized by transmission electron microscopy (TEM) and x-ray energy dispersive spectrometer (EDS). The sheet-shaped single-crystalline nanostructures are pure rutile-phase structure, with landscape dimension of 10-45 nm. EDS investigation confirms that the TiO2 nanosheets are only composed of Ti and O, and the atomic ration of Ti and O is close to 1:2. High photocatalytic activity might be expected for those TiO2 nanosheets due to their large surface area.

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